Diethylamine → HCID 14716807, compound

HRID 1655139Notes

Reaction equation

HRID 1655139 reaction equation
I[C:2]1[CH:7]=[CH:6][C:5](I)=[CH:4][CH:3]=1.C(N[CH2:12][CH3:13])C.[CH2:14]([C:17]1[CH:22]=[CH:21][C:20]([C:23]#[CH:24])=[CH:19][CH:18]=1)[CH2:15][CH3:16]>[Cu](I)I.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.O>[CH2:21]([C:2]1[CH:7]=[CH:6][C:5]([C:24]#[C:23][C:20]2[CH:19]=[CH:18][C:17]([C:14]#[C:15][C:16]3[CH:19]=[CH:18][C:17]([CH2:22][CH2:12][CH3:13])=[CH:14][CH:15]=3)=[CH:22][CH:21]=2)=[CH:4][CH:3]=1)[CH2:20][CH3:23]

Participants

7

Procedure

1,4-Diiodobenzene (2.5 g, 7.57 mmol) was added to diethylamine (80 ml) in nitrogen gas stream, followed by agitating the mixture at room temperature, successively adding copper iodide (60 mg) and dichlorobis(triphenylphosphine)palladium(II) (100 mg), adding 4-propylphenylacetylene (4.37 g, 30 mmol) in several steps, agitating the reaction mixture at room temperature overnight, adding water (200 ml), extracting the resulting deposited crystals with toluene (100 ml), washing the toluene solution with dilute hydrochloric acid, water, an aqueous solution of sodium hydrogen sulfate and water in this order, drying the solution on anhydrous sodium sulfate, passing it through a short column of activated alumina, distilling off toluene and recrystallizing the residue from ethyl acetate to obtain the objective 1,4-bis-(4-propylphenyl-ethynyl)benzene (1.92 g, 5.3 mmol). This product exhibited liquid crystal phases. C-N point: 179.1° C. N-I point: 245.5° C.

Workup

  1. stirringagitating the reaction mixture at room temperature overnight
  2. extractionextracting the resulting
  3. washwashing the toluene solution with dilute hydrochloric acid, water
  4. dry with materialan aqueous solution of sodium hydrogen sulfate and water in this order, drying the solution on anhydrous sodium sulfate
  5. distillationdistilling off toluene
  6. customrecrystallizing the residue from ethyl acetate

Sources & evidence

ORD record
ord-ac8d1be914834fbd90fab20fe68ec7cf
Source dataset
uspto-grants-1993_10
Patent number
US05250216

Reaction notes

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